Which of the following statements justifies why LiAIH, is a more powerful reducing agent than its...
8. Which of the following statements justifies why LiAlHs is a more powerful reducing agent than its isoelectronic counterpart NaBH4? i. NaH is a strong nucleophile, meaning the direct attachment of the hydride to li. The dipole moment of LiAIHs is higher than that of NaBHa, making its hydride ii. NaBHs is just as much of a strong reducing agent, with the ability to reduce a the sodium ion will make the hydride more nucleophilic like LiAIH more nucleophilic. nitrile...
1. Matching. For each functional group on the left, select the reducing agent(s) on the right that WILL successfully react with the given functional group. Write the letter that corresponds to the correct answer on the line next to the functional group. once, and you may or may not use all of the possible answers. (5 pts) You will use one or more of the answers more than carboxylic acid a) LiAIH b) NaBH c) both LiAlH4 and NaBH4 d)...